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Compare the effects of isosorbide mono nitrate and misoprostol for cervical ripening for labor in term pregnancy

Compare the effects of isosorbide mono nitrate and misoprostol for cervical ripening for labor in term pregnancy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017031233025N1
Enrollment
50
Registered
2017-04-12
Start date
2016-03-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Term pergnancy.

Interventions

Intervention 1: 40 mg Isosorbide Mononitrate will be given ever 6 hours in 3 dose At intervals of 0, 6 and 12 hours. Intervention 2: 25 µg misoprostol will be given ever 6 hours in 3 dose At interva
Treatment - Drugs
40 mg Isosorbide Mononitrate will be given ever 6 hours in 3 dose At intervals of 0, 6 and 12 hours.
25 µg misoprostol will be given ever 6 hours in 3 dose At intervals of 0, 6 and 12 hours.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: term pregnancy having indication for termination; Bishop score less than 6; not using another method for cervical ripening. Exclusion criteria: preterm pregnancies; Bishop-score of 6; coagulation disorder; Cesarean section; severe preeclampsia; primary hypo tension; any type of heart disease; using any medication for heart disease, anticoagulants, contortionists and history for adrenal disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Apgar score. Timepoint: after intervention. Method of measurement: According to expert examination.

Secondary

MeasureTime frame
Bishop Scale. Timepoint: After intervention. Method of measurement: According to expert examination.;Effective time. Timepoint: After intervention. Method of measurement: Hours.;Hypertension et contractions. Timepoint: After intervention. Method of measurement: According to expert examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Lotfalizade

Mashhad University of Medical Sciences

lotfalizadem@mums.ac.ir+98 51 3802 2608

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026